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rs786205798

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205798(-;-)
Make rs786205798(-;T)
Make rs786205798(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position115701423
GeneCASQ2
is asnp
is mentioned by
dbSNPrs786205798
ebirs786205798
HLIrs786205798
Exacrs786205798
Varsomers786205798
Maprs786205798
PheGenIrs786205798
hapmaprs786205798
1000 genomesrs786205798
hgdprs786205798
ensemblrs786205798
gopubmedrs786205798
geneviewrs786205798
scholarrs786205798
googlers786205798
pharmgkbrs786205798
gwascentralrs786205798
openSNPrs786205798
23andMers786205798
23andMe allrs786205798
SNP Nexus

SNPshotrs786205798
SNPdbers786205798
MSV3drs786205798
GWAS Ctlgrs786205798
Max Magnitude0
ClinVar
Risk rs786205798(T;T)
Alt rs786205798(T;T)
Reference rs786205798(;)
Significance Pathogenic
Disease not provided
Variation info
Gene CASQ2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.116244045dupA
CLNSRC
CLNACC RCV000170913.3,