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rs1057517715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517715(C;T)
Make rs1057517715(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position85911292
GeneCHM
is asnp
is mentioned by
dbSNPrs1057517715
dbSNP (old)rs1057517715
ClinGenrs1057517715
ebirs1057517715
HLIrs1057517715
Exacrs1057517715
Gnomadrs1057517715
Varsomers1057517715
LitVarrs1057517715
Maprs1057517715
PheGenIrs1057517715
Biobankrs1057517715
1000 genomesrs1057517715
hgdprs1057517715
ensemblrs1057517715
gopubmedrs1057517715
geneviewrs1057517715
scholarrs1057517715
googlers1057517715
pharmgkbrs1057517715
gwascentralrs1057517715
openSNPrs1057517715
23andMers1057517715
23andMe allrs1057517715
SNPshotrs1057517715
SNPdbers1057517715
MSV3drs1057517715
GWAS Ctlgrs1057517715
Max Magnitude0
ClinVar
Risk rs1057517715(T;T)
Alt rs1057517715(T;T)
Reference Rs1057517715(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85166297G>A
CLNSRC
CLNACC RCV000413451.1,