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rs786205792

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205792(C;C)
Make rs786205792(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position115701359
GeneCASQ2
is asnp
is mentioned by
dbSNPrs786205792
ebirs786205792
HLIrs786205792
Exacrs786205792
Varsomers786205792
Maprs786205792
PheGenIrs786205792
hapmaprs786205792
1000 genomesrs786205792
hgdprs786205792
ensemblrs786205792
gopubmedrs786205792
geneviewrs786205792
scholarrs786205792
googlers786205792
pharmgkbrs786205792
gwascentralrs786205792
openSNPrs786205792
23andMers786205792
23andMe allrs786205792
SNP Nexus

SNPshotrs786205792
SNPdbers786205792
MSV3drs786205792
GWAS Ctlgrs786205792
Max Magnitude0
ClinVar
Risk rs786205792(C;C)
Alt rs786205792(C;C)
Reference rs786205792(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASQ2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.116243980C>G
CLNSRC
CLNACC RCV000170896.3,