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rs886041181

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position85956181
GeneCHM
is asnp
is mentioned by
dbSNPrs886041181
dbSNP (classic)rs886041181
ClinGenrs886041181
ebirs886041181
HLIrs886041181
Exacrs886041181
Gnomadrs886041181
Varsomers886041181
LitVarrs886041181
Maprs886041181
PheGenIrs886041181
Biobankrs886041181
1000 genomesrs886041181
hgdprs886041181
ensemblrs886041181
geneviewrs886041181
scholarrs886041181
googlers886041181
pharmgkbrs886041181
gwascentralrs886041181
openSNPrs886041181
23andMers886041181
23andMe allrs886041181
SNPshotrs886041181
SNPdbers886041181
MSV3drs886041181
GWAS Ctlgrs886041181
Max Magnitude0
ClinVar
Risk rs886041181(T;T)
Alt rs886041181(T;T)
Reference Rs886041181(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85211186G>A
CLNSRC
CLNACC RCV000285432.1,