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rs750459631

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs750459631(G;G)
Make rs750459631(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position162101232
GeneGABRG2
is asnp
is mentioned by
dbSNPrs750459631
ebirs750459631
HLIrs750459631
Exacrs750459631
Varsomers750459631
Maprs750459631
PheGenIrs750459631
hapmaprs750459631
1000 genomesrs750459631
hgdprs750459631
ensemblrs750459631
gopubmedrs750459631
geneviewrs750459631
scholarrs750459631
googlers750459631
pharmgkbrs750459631
gwascentralrs750459631
openSNPrs750459631
23andMers750459631
23andMe allrs750459631
SNP Nexus

SNPshotrs750459631
SNPdbers750459631
MSV3drs750459631
GWAS Ctlgrs750459631
Max Magnitude0
ClinVar
Risk rs750459631(G;G)
Alt rs750459631(G;G)
Reference rs750459631(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161528238T>G
CLNSRC
CLNACC RCV000187524.1,