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rs776996552

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776996552(C;T)
Make rs776996552(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position38343441
GeneGPR179
is asnp
is mentioned by
dbSNPrs776996552
ebirs776996552
HLIrs776996552
Exacrs776996552
Varsomers776996552
Maprs776996552
PheGenIrs776996552
hapmaprs776996552
1000 genomesrs776996552
hgdprs776996552
ensemblrs776996552
gopubmedrs776996552
geneviewrs776996552
scholarrs776996552
googlers776996552
pharmgkbrs776996552
gwascentralrs776996552
openSNPrs776996552
23andMers776996552
23andMe allrs776996552
SNP Nexus

SNPshotrs776996552
SNPdbers776996552
MSV3drs776996552
GWAS Ctlgrs776996552
Max Magnitude0
ClinVar
Risk rs776996552(T;T)
Alt rs776996552(T;T)
Reference rs776996552(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GPR179
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.36499324C>T
CLNSRC
CLNACC RCV000171255.1,