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rs762381137

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs762381137(A;G)
Make rs762381137(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position115717869
GeneCASQ2
is asnp
is mentioned by
dbSNPrs762381137
ebirs762381137
HLIrs762381137
Exacrs762381137
Varsomers762381137
Maprs762381137
PheGenIrs762381137
hapmaprs762381137
1000 genomesrs762381137
hgdprs762381137
ensemblrs762381137
gopubmedrs762381137
geneviewrs762381137
scholarrs762381137
googlers762381137
pharmgkbrs762381137
gwascentralrs762381137
openSNPrs762381137
23andMers762381137
23andMe allrs762381137
SNP Nexus

SNPshotrs762381137
SNPdbers762381137
MSV3drs762381137
GWAS Ctlgrs762381137
Max Magnitude0
ClinVar
Risk rs762381137(G;G)
Alt rs762381137(G;G)
Reference rs762381137(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASQ2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.116260490A>G
CLNSRC
CLNACC RCV000170892.2,