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rs201977531

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201977531(A;G)
Make rs201977531(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position160134547
GeneATP1A2
is asnp
is mentioned by
dbSNPrs201977531
ebirs201977531
HLIrs201977531
Exacrs201977531
Varsomers201977531
Maprs201977531
PheGenIrs201977531
hapmaprs201977531
1000 genomesrs201977531
hgdprs201977531
ensemblrs201977531
gopubmedrs201977531
geneviewrs201977531
scholarrs201977531
googlers201977531
pharmgkbrs201977531
gwascentralrs201977531
openSNPrs201977531
23andMers201977531
23andMe allrs201977531
SNP Nexus

SNPshotrs201977531
SNPdbers201977531
MSV3drs201977531
GWAS Ctlgrs201977531
Max Magnitude0
ClinVar
Risk rs201977531(G;G)
Alt rs201977531(G;G)
Reference rs201977531(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP1A2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.160104337A>G
CLNSRC
CLNACC RCV000186795.2,