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rs767983680

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767983680(C;G)
Make rs767983680(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position1204058
GeneCACNA1H
is asnp
is mentioned by
dbSNPrs767983680
dbSNP (classic)rs767983680
ClinGenrs767983680
ebirs767983680
HLIrs767983680
Exacrs767983680
Gnomadrs767983680
Varsomers767983680
LitVarrs767983680
Maprs767983680
PheGenIrs767983680
Biobankrs767983680
1000 genomesrs767983680
hgdprs767983680
ensemblrs767983680
geneviewrs767983680
scholarrs767983680
googlers767983680
pharmgkbrs767983680
gwascentralrs767983680
openSNPrs767983680
23andMers767983680
SNPshotrs767983680
SNPdbers767983680
MSV3drs767983680
GWAS Ctlgrs767983680
Max Magnitude0
ClinVar
Risk rs767983680(A;A) rs767983680(G;G)
Alt rs767983680(A;A) rs767983680(G;G)
Reference Rs767983680(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene CACNA1H
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000016.9:g.1254058C>A
CLNSRC
CLNACC RCV000454200.1,