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rs886041178

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position85958923
GeneCHM
is asnp
is mentioned by
dbSNPrs886041178
dbSNP (classic)rs886041178
ClinGenrs886041178
ebirs886041178
HLIrs886041178
Exacrs886041178
Gnomadrs886041178
Varsomers886041178
LitVarrs886041178
Maprs886041178
PheGenIrs886041178
Biobankrs886041178
1000 genomesrs886041178
hgdprs886041178
ensemblrs886041178
geneviewrs886041178
scholarrs886041178
googlers886041178
pharmgkbrs886041178
gwascentralrs886041178
openSNPrs886041178
23andMers886041178
23andMe allrs886041178
SNPshotrs886041178
SNPdbers886041178
MSV3drs886041178
GWAS Ctlgrs886041178
Max Magnitude0
ClinVar
Risk rs886041178(A;A) rs886041178(T;T)
Alt rs886041178(A;A) rs886041178(T;T)
Reference Rs886041178(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85213928G>A
CLNSRC
CLNACC RCV000265578.1,