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rs886041179

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position85958881
GeneCHM
is asnp
is mentioned by
dbSNPrs886041179
dbSNP (classic)rs886041179
ClinGenrs886041179
ebirs886041179
HLIrs886041179
Exacrs886041179
Gnomadrs886041179
Varsomers886041179
LitVarrs886041179
Maprs886041179
PheGenIrs886041179
Biobankrs886041179
1000 genomesrs886041179
hgdprs886041179
ensemblrs886041179
geneviewrs886041179
scholarrs886041179
googlers886041179
pharmgkbrs886041179
gwascentralrs886041179
openSNPrs886041179
23andMers886041179
23andMe allrs886041179
SNPshotrs886041179
SNPdbers886041179
MSV3drs886041179
GWAS Ctlgrs886041179
Max Magnitude0
ClinVar
Risk rs886041179(T;T)
Alt rs886041179(T;T)
Reference Rs886041179(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85213886G>A
CLNSRC
CLNACC RCV000320612.1,