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rs886041402

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position80182791
GeneCARD14
is asnp
is mentioned by
dbSNPrs886041402
dbSNP (classic)rs886041402
ClinGenrs886041402
ebirs886041402
HLIrs886041402
Exacrs886041402
Gnomadrs886041402
Varsomers886041402
LitVarrs886041402
Maprs886041402
PheGenIrs886041402
Biobankrs886041402
1000 genomesrs886041402
hgdprs886041402
ensemblrs886041402
geneviewrs886041402
scholarrs886041402
googlers886041402
pharmgkbrs886041402
gwascentralrs886041402
openSNPrs886041402
23andMers886041402
SNPshotrs886041402
SNPdbers886041402
MSV3drs886041402
GWAS Ctlgrs886041402
Max Magnitude0
ClinVar
Risk rs886041402(A;A)
Alt rs886041402(A;A)
Reference Rs886041402(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CARD14
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.78156590G>A
CLNSRC
CLNACC RCV000262256.1,