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rs772685782

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772685782(A;A)
Make rs772685782(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position50591539
GeneCACNA1G
is asnp
is mentioned by
dbSNPrs772685782
dbSNP (classic)rs772685782
ClinGenrs772685782
ebirs772685782
HLIrs772685782
Exacrs772685782
Gnomadrs772685782
Varsomers772685782
LitVarrs772685782
Maprs772685782
PheGenIrs772685782
Biobankrs772685782
1000 genomesrs772685782
hgdprs772685782
ensemblrs772685782
geneviewrs772685782
scholarrs772685782
googlers772685782
pharmgkbrs772685782
gwascentralrs772685782
openSNPrs772685782
23andMers772685782
SNPshotrs772685782
SNPdbers772685782
MSV3drs772685782
GWAS Ctlgrs772685782
Max Magnitude0
ClinVar
Risk rs772685782(A;A)
Alt rs772685782(A;A)
Reference Rs772685782(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CACNA1G
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.48668900G>A
CLNSRC
CLNACC RCV000493653.1,