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rs786205604

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205604(G;T)
Make rs786205604(T;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position85956175
GeneCHM
is asnp
is mentioned by
dbSNPrs786205604
ebirs786205604
HLIrs786205604
Exacrs786205604
Varsomers786205604
Maprs786205604
PheGenIrs786205604
hapmaprs786205604
1000 genomesrs786205604
hgdprs786205604
ensemblrs786205604
gopubmedrs786205604
geneviewrs786205604
scholarrs786205604
googlers786205604
pharmgkbrs786205604
gwascentralrs786205604
openSNPrs786205604
23andMers786205604
23andMe allrs786205604
SNP Nexus

SNPshotrs786205604
SNPdbers786205604
MSV3drs786205604
GWAS Ctlgrs786205604
Max Magnitude0
ClinVar
Risk rs786205604(T;T)
Alt rs786205604(T;T)
Reference rs786205604(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85211180C>A
CLNSRC
CLNACC RCV000171441.1,