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rs1048609704

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position130980606
GeneATP2C1
is asnp
is mentioned by
dbSNPrs1048609704
dbSNP (old)rs1048609704
ClinGenrs1048609704
ebirs1048609704
HLIrs1048609704
Exacrs1048609704
Gnomadrs1048609704
Varsomers1048609704
Maprs1048609704
PheGenIrs1048609704
Biobankrs1048609704
1000 genomesrs1048609704
hgdprs1048609704
ensemblrs1048609704
gopubmedrs1048609704
geneviewrs1048609704
scholarrs1048609704
googlers1048609704
pharmgkbrs1048609704
gwascentralrs1048609704
openSNPrs1048609704
23andMers1048609704
23andMe allrs1048609704
SNPshotrs1048609704
SNPdbers1048609704
MSV3drs1048609704
GWAS Ctlgrs1048609704
Max Magnitude0
ClinVar
Risk rs1048609704(G;G)
Alt rs1048609704(G;G)
Reference Rs1048609704(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.130699450A>G
CLNSRC
CLNACC RCV000484022.1,