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rs796052491

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052491(C;C)
Make rs796052491(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position161890982
GeneGABRA1
is asnp
is mentioned by
dbSNPrs796052491
ebirs796052491
HLIrs796052491
Exacrs796052491
Varsomers796052491
Maprs796052491
PheGenIrs796052491
hapmaprs796052491
1000 genomesrs796052491
hgdprs796052491
ensemblrs796052491
gopubmedrs796052491
geneviewrs796052491
scholarrs796052491
googlers796052491
pharmgkbrs796052491
gwascentralrs796052491
openSNPrs796052491
23andMers796052491
23andMe allrs796052491
SNP Nexus

SNPshotrs796052491
SNPdbers796052491
MSV3drs796052491
GWAS Ctlgrs796052491
Max Magnitude0
ClinVar
Risk rs796052491(C;C)
Alt rs796052491(C;C)
Reference rs796052491(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GABRA1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161317988T>C
CLNSRC
CLNACC RCV000187499.2,