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rs1057520476

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520476(A;A)
Make rs1057520476(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position162097850
GeneGABRG2
is asnp
is mentioned by
dbSNPrs1057520476
dbSNP (classic)rs1057520476
ClinGenrs1057520476
ebirs1057520476
HLIrs1057520476
Exacrs1057520476
Gnomadrs1057520476
Varsomers1057520476
LitVarrs1057520476
Maprs1057520476
PheGenIrs1057520476
Biobankrs1057520476
1000 genomesrs1057520476
hgdprs1057520476
ensemblrs1057520476
geneviewrs1057520476
scholarrs1057520476
googlers1057520476
pharmgkbrs1057520476
gwascentralrs1057520476
openSNPrs1057520476
23andMers1057520476
23andMe allrs1057520476
SNPshotrs1057520476
SNPdbers1057520476
MSV3drs1057520476
GWAS Ctlgrs1057520476
Max Magnitude0
ClinVar
Risk rs1057520476(A;A)
Alt rs1057520476(A;A)
Reference Rs1057520476(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161524856C>A
CLNSRC
CLNACC RCV000418335.1,