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rs1057518594

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518594(-;A)
Make rs1057518594(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position130997697
GeneATP2C1
is asnp
is mentioned by
dbSNPrs1057518594
dbSNP (old)rs1057518594
ClinGenrs1057518594
ebirs1057518594
HLIrs1057518594
Exacrs1057518594
Gnomadrs1057518594
Varsomers1057518594
Maprs1057518594
PheGenIrs1057518594
Biobankrs1057518594
1000 genomesrs1057518594
hgdprs1057518594
ensemblrs1057518594
gopubmedrs1057518594
geneviewrs1057518594
scholarrs1057518594
googlers1057518594
pharmgkbrs1057518594
gwascentralrs1057518594
openSNPrs1057518594
23andMers1057518594
23andMe allrs1057518594
SNPshotrs1057518594
SNPdbers1057518594
MSV3drs1057518594
GWAS Ctlgrs1057518594
Max Magnitude0
ClinVar
Risk rs1057518594(A;A)
Alt rs1057518594(A;A)
Reference Rs1057518594(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP2C1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.130716541dupA
CLNSRC
CLNACC RCV000413901.1,