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rs886041176

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCAG;TCAG) 0 common in clinvar
ChromosomeX
Position85964049
GeneCHM
is asnp
is mentioned by
dbSNPrs886041176
dbSNP (classic)rs886041176
ClinGenrs886041176
ebirs886041176
HLIrs886041176
Exacrs886041176
Gnomadrs886041176
Varsomers886041176
LitVarrs886041176
Maprs886041176
PheGenIrs886041176
Biobankrs886041176
1000 genomesrs886041176
hgdprs886041176
ensemblrs886041176
geneviewrs886041176
scholarrs886041176
googlers886041176
pharmgkbrs886041176
gwascentralrs886041176
openSNPrs886041176
23andMers886041176
23andMe allrs886041176
SNPshotrs886041176
SNPdbers886041176
MSV3drs886041176
GWAS Ctlgrs886041176
Max Magnitude0
ClinVar
Risk rs886041176(-;-)
Alt rs886041176(-;-)
Reference Rs886041176(TCAG;TCAG)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85219054_85219057delCTGA
CLNSRC
CLNACC RCV000319155.2,