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rs886041174

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position86047483
GeneCHM
is asnp
is mentioned by
dbSNPrs886041174
dbSNP (classic)rs886041174
ClinGenrs886041174
ebirs886041174
HLIrs886041174
Exacrs886041174
Gnomadrs886041174
Varsomers886041174
LitVarrs886041174
Maprs886041174
PheGenIrs886041174
Biobankrs886041174
1000 genomesrs886041174
hgdprs886041174
ensemblrs886041174
geneviewrs886041174
scholarrs886041174
googlers886041174
pharmgkbrs886041174
gwascentralrs886041174
openSNPrs886041174
23andMers886041174
23andMe allrs886041174
SNPshotrs886041174
SNPdbers886041174
MSV3drs886041174
GWAS Ctlgrs886041174
Max Magnitude0
ClinVar
Risk rs886041174(T;T)
Alt rs886041174(T;T)
Reference Rs886041174(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85302487C>A
CLNSRC
CLNACC RCV000313760.1,