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rs796052515

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052515(C;T)
Make rs796052515(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162153300
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052515
ebirs796052515
HLIrs796052515
Exacrs796052515
Varsomers796052515
Maprs796052515
PheGenIrs796052515
hapmaprs796052515
1000 genomesrs796052515
hgdprs796052515
ensemblrs796052515
gopubmedrs796052515
geneviewrs796052515
scholarrs796052515
googlers796052515
pharmgkbrs796052515
gwascentralrs796052515
openSNPrs796052515
23andMers796052515
23andMe allrs796052515
SNP Nexus

SNPshotrs796052515
SNPdbers796052515
MSV3drs796052515
GWAS Ctlgrs796052515
Max Magnitude0
ClinVar
Risk rs796052515(T;T)
Alt rs796052515(T;T)
Reference rs796052515(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161580306C>T
CLNSRC
CLNACC RCV000187538.2,