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rs886041177

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
ChromosomeX
Position85963841
GeneCHM
is asnp
is mentioned by
dbSNPrs886041177
dbSNP (classic)rs886041177
ClinGenrs886041177
ebirs886041177
HLIrs886041177
Exacrs886041177
Gnomadrs886041177
Varsomers886041177
LitVarrs886041177
Maprs886041177
PheGenIrs886041177
Biobankrs886041177
1000 genomesrs886041177
hgdprs886041177
ensemblrs886041177
geneviewrs886041177
scholarrs886041177
googlers886041177
pharmgkbrs886041177
gwascentralrs886041177
openSNPrs886041177
23andMers886041177
23andMe allrs886041177
SNPshotrs886041177
SNPdbers886041177
MSV3drs886041177
GWAS Ctlgrs886041177
Max Magnitude0
ClinVar
Risk rs886041177(-;-)
Alt rs886041177(-;-)
Reference Rs886041177(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85218846_85218847delCT
CLNSRC
CLNACC RCV000355316.1,