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rs1057517716

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517716(C;T)
Make rs1057517716(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position85901091
GeneCHM
is asnp
is mentioned by
dbSNPrs1057517716
dbSNP (old)rs1057517716
ClinGenrs1057517716
ebirs1057517716
HLIrs1057517716
Exacrs1057517716
Gnomadrs1057517716
Varsomers1057517716
Maprs1057517716
PheGenIrs1057517716
Biobankrs1057517716
1000 genomesrs1057517716
hgdprs1057517716
ensemblrs1057517716
gopubmedrs1057517716
geneviewrs1057517716
scholarrs1057517716
googlers1057517716
pharmgkbrs1057517716
gwascentralrs1057517716
openSNPrs1057517716
23andMers1057517716
23andMe allrs1057517716
SNPshotrs1057517716
SNPdbers1057517716
MSV3drs1057517716
GWAS Ctlgrs1057517716
Max Magnitude0
ClinVar
Risk rs1057517716(T;T)
Alt rs1057517716(T;T)
Reference Rs1057517716(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85156096G>A
CLNSRC
CLNACC RCV000414063.1,