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rs1057520629

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520629(C;G)
Make rs1057520629(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position85901099
GeneCHM
is asnp
is mentioned by
dbSNPrs1057520629
dbSNP (old)rs1057520629
ClinGenrs1057520629
ebirs1057520629
HLIrs1057520629
Exacrs1057520629
Gnomadrs1057520629
Varsomers1057520629
Maprs1057520629
PheGenIrs1057520629
Biobankrs1057520629
1000 genomesrs1057520629
hgdprs1057520629
ensemblrs1057520629
gopubmedrs1057520629
geneviewrs1057520629
scholarrs1057520629
googlers1057520629
pharmgkbrs1057520629
gwascentralrs1057520629
openSNPrs1057520629
23andMers1057520629
23andMe allrs1057520629
SNPshotrs1057520629
SNPdbers1057520629
MSV3drs1057520629
GWAS Ctlgrs1057520629
Max Magnitude0
ClinVar
Risk rs1057520629(G;G)
Alt rs1057520629(G;G)
Reference Rs1057520629(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85156104G>C
CLNSRC
CLNACC RCV000431379.1,