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rs886041175

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position85981796
GeneCHM
is asnp
is mentioned by
dbSNPrs886041175
dbSNP (classic)rs886041175
ClinGenrs886041175
ebirs886041175
HLIrs886041175
Exacrs886041175
Gnomadrs886041175
Varsomers886041175
LitVarrs886041175
Maprs886041175
PheGenIrs886041175
Biobankrs886041175
1000 genomesrs886041175
hgdprs886041175
ensemblrs886041175
geneviewrs886041175
scholarrs886041175
googlers886041175
pharmgkbrs886041175
gwascentralrs886041175
openSNPrs886041175
23andMers886041175
23andMe allrs886041175
SNPshotrs886041175
SNPdbers886041175
MSV3drs886041175
GWAS Ctlgrs886041175
Max Magnitude0
ClinVar
Risk rs886041175(T;T)
Alt rs886041175(T;T)
Reference Rs886041175(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85236800C>A
CLNSRC
CLNACC RCV000259262.1,