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rs786205753

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205753(A;A)
Make rs786205753(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position2593255
GeneCACNA1C
is asnp
is mentioned by
dbSNPrs786205753
ebirs786205753
HLIrs786205753
Exacrs786205753
Varsomers786205753
Maprs786205753
PheGenIrs786205753
hapmaprs786205753
1000 genomesrs786205753
hgdprs786205753
ensemblrs786205753
gopubmedrs786205753
geneviewrs786205753
scholarrs786205753
googlers786205753
pharmgkbrs786205753
gwascentralrs786205753
openSNPrs786205753
23andMers786205753
23andMe allrs786205753
SNP Nexus

SNPshotrs786205753
SNPdbers786205753
MSV3drs786205753
GWAS Ctlgrs786205753
Max Magnitude0
ClinVar
Risk rs786205753(A;A)
Alt rs786205753(A;A)
Reference rs786205753(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CACNA1C
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.2702421G>A
CLNSRC
CLNACC RCV000170791.3,