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rs767121010

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767121010(A;A)
Make rs767121010(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position50626566
GeneCACNA1G, LOC101927253
is asnp
is mentioned by
dbSNPrs767121010
dbSNP (classic)rs767121010
ClinGenrs767121010
ebirs767121010
HLIrs767121010
Exacrs767121010
Gnomadrs767121010
Varsomers767121010
LitVarrs767121010
Maprs767121010
PheGenIrs767121010
Biobankrs767121010
1000 genomesrs767121010
hgdprs767121010
ensemblrs767121010
geneviewrs767121010
scholarrs767121010
googlers767121010
pharmgkbrs767121010
gwascentralrs767121010
openSNPrs767121010
23andMers767121010
SNPshotrs767121010
SNPdbers767121010
MSV3drs767121010
GWAS Ctlgrs767121010
Max Magnitude0
ClinVar
Risk rs767121010(A;A)
Alt rs767121010(A;A)
Reference Rs767121010(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101927253 CACNA1G
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.48703927G>A
CLNSRC
CLNACC RCV000489205.1,