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rs886041180

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position85956350
GeneCHM
is asnp
is mentioned by
dbSNPrs886041180
dbSNP (classic)rs886041180
ClinGenrs886041180
ebirs886041180
HLIrs886041180
Exacrs886041180
Gnomadrs886041180
Varsomers886041180
LitVarrs886041180
Maprs886041180
PheGenIrs886041180
Biobankrs886041180
1000 genomesrs886041180
hgdprs886041180
ensemblrs886041180
geneviewrs886041180
scholarrs886041180
googlers886041180
pharmgkbrs886041180
gwascentralrs886041180
openSNPrs886041180
23andMers886041180
23andMe allrs886041180
SNPshotrs886041180
SNPdbers886041180
MSV3drs886041180
GWAS Ctlgrs886041180
Max Magnitude0
ClinVar
Risk rs886041180(A;A)
Alt rs886041180(A;A)
Reference Rs886041180(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85211355A>T
CLNSRC
CLNACC RCV000379861.1,