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rs1057517717

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517717(-;A)
Make rs1057517717(A;A)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position85894260
GeneCHM
is asnp
is mentioned by
dbSNPrs1057517717
dbSNP (classic)rs1057517717
ClinGenrs1057517717
ebirs1057517717
HLIrs1057517717
Exacrs1057517717
Gnomadrs1057517717
Varsomers1057517717
LitVarrs1057517717
Maprs1057517717
PheGenIrs1057517717
Biobankrs1057517717
1000 genomesrs1057517717
hgdprs1057517717
ensemblrs1057517717
geneviewrs1057517717
scholarrs1057517717
googlers1057517717
pharmgkbrs1057517717
gwascentralrs1057517717
openSNPrs1057517717
23andMers1057517717
23andMe allrs1057517717
SNPshotrs1057517717
SNPdbers1057517717
MSV3drs1057517717
GWAS Ctlgrs1057517717
Max Magnitude0
ClinVar
Risk rs1057517717(A;A)
Alt rs1057517717(A;A)
Reference Rs1057517717(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85149266dupT
CLNSRC
CLNACC RCV000412929.1,