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rs1057521475

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521475(A;A)
Make rs1057521475(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position86047479
GeneCHM
is asnp
is mentioned by
dbSNPrs1057521475
dbSNP (old)rs1057521475
ClinGenrs1057521475
ebirs1057521475
HLIrs1057521475
Exacrs1057521475
Gnomadrs1057521475
Varsomers1057521475
LitVarrs1057521475
Maprs1057521475
PheGenIrs1057521475
Biobankrs1057521475
1000 genomesrs1057521475
hgdprs1057521475
ensemblrs1057521475
gopubmedrs1057521475
geneviewrs1057521475
scholarrs1057521475
googlers1057521475
pharmgkbrs1057521475
gwascentralrs1057521475
openSNPrs1057521475
23andMers1057521475
23andMe allrs1057521475
SNPshotrs1057521475
SNPdbers1057521475
MSV3drs1057521475
GWAS Ctlgrs1057521475
Max Magnitude0
ClinVar
Risk rs1057521475(A;A)
Alt rs1057521475(A;A)
Reference Rs1057521475(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.85302483C>T
CLNSRC
CLNACC RCV000419936.1,