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rs1057520634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520634(C;T)
Make rs1057520634(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position130996750
GeneATP2C1
is asnp
is mentioned by
dbSNPrs1057520634
dbSNP (classic)rs1057520634
ClinGenrs1057520634
ebirs1057520634
HLIrs1057520634
Exacrs1057520634
Gnomadrs1057520634
Varsomers1057520634
LitVarrs1057520634
Maprs1057520634
PheGenIrs1057520634
Biobankrs1057520634
1000 genomesrs1057520634
hgdprs1057520634
ensemblrs1057520634
geneviewrs1057520634
scholarrs1057520634
googlers1057520634
pharmgkbrs1057520634
gwascentralrs1057520634
openSNPrs1057520634
23andMers1057520634
23andMe allrs1057520634
SNPshotrs1057520634
SNPdbers1057520634
MSV3drs1057520634
GWAS Ctlgrs1057520634
Max Magnitude0
ClinVar
Risk rs1057520634(T;T)
Alt rs1057520634(T;T)
Reference Rs1057520634(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP2C1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.130715594C>T
CLNSRC
CLNACC RCV000436933.1,