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rs797044881

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044881(C;C)
Make rs797044881(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position2608651
GeneCACNA1C
is asnp
is mentioned by
dbSNPrs797044881
ebirs797044881
HLIrs797044881
Exacrs797044881
Varsomers797044881
Maprs797044881
PheGenIrs797044881
hapmaprs797044881
1000 genomesrs797044881
hgdprs797044881
ensemblrs797044881
gopubmedrs797044881
geneviewrs797044881
scholarrs797044881
googlers797044881
pharmgkbrs797044881
gwascentralrs797044881
openSNPrs797044881
23andMers797044881
23andMe allrs797044881
SNP Nexus

SNPshotrs797044881
SNPdbers797044881
MSV3drs797044881
GWAS Ctlgrs797044881
Max Magnitude0
ClinVar
Risk rs797044881(C;C)
Alt rs797044881(C;C)
Reference rs797044881(T;T)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CACNA1C
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000012.11:g.2717817T>C
CLNSRC
CLNACC RCV000190696.1,