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rs796052276

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052276(C;T)
Make rs796052276(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position160128725
GeneATP1A2
is asnp
is mentioned by
dbSNPrs796052276
ebirs796052276
HLIrs796052276
Exacrs796052276
Varsomers796052276
Maprs796052276
PheGenIrs796052276
hapmaprs796052276
1000 genomesrs796052276
hgdprs796052276
ensemblrs796052276
gopubmedrs796052276
geneviewrs796052276
scholarrs796052276
googlers796052276
pharmgkbrs796052276
gwascentralrs796052276
openSNPrs796052276
23andMers796052276
23andMe allrs796052276
SNP Nexus

SNPshotrs796052276
SNPdbers796052276
MSV3drs796052276
GWAS Ctlgrs796052276
Max Magnitude0
ClinVar
Risk rs796052276(T;T)
Alt rs796052276(T;T)
Reference rs796052276(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP1A2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.160098515C>T
CLNSRC
CLNACC RCV000186786.1,