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rs755310507

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs755310507(A;A)
Make rs755310507(A;C)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position160136307
GeneATP1A2
is asnp
is mentioned by
dbSNPrs755310507
dbSNP (classic)rs755310507
ClinGenrs755310507
ebirs755310507
HLIrs755310507
Exacrs755310507
Gnomadrs755310507
Varsomers755310507
LitVarrs755310507
Maprs755310507
PheGenIrs755310507
Biobankrs755310507
1000 genomesrs755310507
hgdprs755310507
ensemblrs755310507
geneviewrs755310507
scholarrs755310507
googlers755310507
pharmgkbrs755310507
gwascentralrs755310507
openSNPrs755310507
23andMers755310507
23andMe allrs755310507
SNPshotrs755310507
SNPdbers755310507
MSV3drs755310507
GWAS Ctlgrs755310507
Max Magnitude0
ClinVar
Risk rs755310507(A;A) rs755310507(T;T)
Alt rs755310507(A;A) rs755310507(T;T)
Reference Rs755310507(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP1A2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.160106097C>T
CLNSRC
CLNACC RCV000256148.1,