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rs1057520765

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520765(G;T)
Make rs1057520765(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position85981793
GeneCHM
is asnp
is mentioned by
dbSNPrs1057520765
dbSNP (old)rs1057520765
ClinGenrs1057520765
ebirs1057520765
HLIrs1057520765
Exacrs1057520765
Gnomadrs1057520765
Varsomers1057520765
Maprs1057520765
PheGenIrs1057520765
Biobankrs1057520765
1000 genomesrs1057520765
hgdprs1057520765
ensemblrs1057520765
gopubmedrs1057520765
geneviewrs1057520765
scholarrs1057520765
googlers1057520765
pharmgkbrs1057520765
gwascentralrs1057520765
openSNPrs1057520765
23andMers1057520765
23andMe allrs1057520765
SNPshotrs1057520765
SNPdbers1057520765
MSV3drs1057520765
GWAS Ctlgrs1057520765
Max Magnitude0
ClinVar
Risk rs1057520765(T;T)
Alt rs1057520765(T;T)
Reference Rs1057520765(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85236797C>A
CLNSRC
CLNACC RCV000435190.1,