Lurp

Cross-platforn SNP explorer. By Peter D'Adamo, ND


rs1799732

Hard Link
rs1799732 is a snp on gene DRD2 (dopamine receptor D2)

GeneDRD2 Chromosome number Chromosome position
Alleles (transliterated to +) Minor Allele Minor Allele Frequency
Notation -141C Ins/Del Clinical significance Orientation (dbSNP) - (negative/reverse strand)
SNP Function
Deletion
Gene Function
This gene encodes a dopamine receptor. A missense mutation in this gene causes the rare myoclonus dystonia; other mutations have been associated with schizophrenia.
This SNP is reported by one or more services.


23andme V3

REPORTED




23andme V4

REPORTED




23andme V5

REPORTED




Ancestry DNA

NOT REPORTED




Genos Export for Promethease

NOT REPORTED




DSL/ Opus Chip

NOT REPORTED




Opus 23 Curated

CURATED




CLINVAR Curated

NOT CURATED




GWAS Curated

NOT CURATED





MOST RECENT SEARCHES:
rs6316 () | rs6295 (HTR1A) | rs34116584 (AGXT) | rs41307258 (TBX22) | rs6993813 () | rs1495741 (NAT2) | rs10046 (CYP19A1) | rs1801198 (TCN2) | rs17036170 (PPARG) | rs2908004 () | Rs17036170 (PPARG)

MOST FREQUENTLY SEARCHED:
rs429358 (APOE) | rs9939609 (FTO) | rs1799941 (SHBG) | rs1801133 (MTHFR) | rs1801181 (CBS) | rs4680 (COMT) | rs6025 (F5) | rs20541 (IL13) | rs2569191 (CD14) | rs2235544 (DIO1) | rs2187668 (HLA-DQA1)








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