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rs1057517714

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517714(A;A)
Make rs1057517714(A;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position85956300
GeneCHM
is asnp
is mentioned by
dbSNPrs1057517714
dbSNP (old)rs1057517714
ClinGenrs1057517714
ebirs1057517714
HLIrs1057517714
Exacrs1057517714
Gnomadrs1057517714
Varsomers1057517714
Maprs1057517714
PheGenIrs1057517714
Biobankrs1057517714
1000 genomesrs1057517714
hgdprs1057517714
ensemblrs1057517714
gopubmedrs1057517714
geneviewrs1057517714
scholarrs1057517714
googlers1057517714
pharmgkbrs1057517714
gwascentralrs1057517714
openSNPrs1057517714
23andMers1057517714
23andMe allrs1057517714
SNPshotrs1057517714
SNPdbers1057517714
MSV3drs1057517714
GWAS Ctlgrs1057517714
Max Magnitude0
ClinVar
Risk rs1057517714(A;A)
Alt rs1057517714(A;A)
Reference Rs1057517714(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85211305G>T
CLNSRC
CLNACC RCV000414588.1,