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rs768061156

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768061156(G;T)
Make rs768061156(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position162149170
GeneGABRG2
is asnp
is mentioned by
dbSNPrs768061156
ebirs768061156
HLIrs768061156
Exacrs768061156
Varsomers768061156
Maprs768061156
PheGenIrs768061156
hapmaprs768061156
1000 genomesrs768061156
hgdprs768061156
ensemblrs768061156
gopubmedrs768061156
geneviewrs768061156
scholarrs768061156
googlers768061156
pharmgkbrs768061156
gwascentralrs768061156
openSNPrs768061156
23andMers768061156
23andMe allrs768061156
SNP Nexus

SNPshotrs768061156
SNPdbers768061156
MSV3drs768061156
GWAS Ctlgrs768061156
Max Magnitude0
ClinVar
Risk rs768061156(T;T)
Alt rs768061156(T;T)
Reference rs768061156(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene GABRG2
CLNDBN not specified
Reversed 0
HGVS NC_000005.9:g.161576176G>T
CLNSRC
CLNACC RCV000187532.3,