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rs1057520298

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520298(A;A)
Make rs1057520298(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position64921812
GeneZC4H2
is asnp
is mentioned by
dbSNPrs1057520298
dbSNP (old)rs1057520298
ClinGenrs1057520298
ebirs1057520298
HLIrs1057520298
Exacrs1057520298
Gnomadrs1057520298
Varsomers1057520298
LitVarrs1057520298
Maprs1057520298
PheGenIrs1057520298
Biobankrs1057520298
1000 genomesrs1057520298
hgdprs1057520298
ensemblrs1057520298
gopubmedrs1057520298
geneviewrs1057520298
scholarrs1057520298
googlers1057520298
pharmgkbrs1057520298
gwascentralrs1057520298
openSNPrs1057520298
23andMers1057520298
23andMe allrs1057520298
SNPshotrs1057520298
SNPdbers1057520298
MSV3drs1057520298
GWAS Ctlgrs1057520298
Max Magnitude0
ClinVar
Risk rs1057520298(A;A) rs1057520298(C;C)
Alt rs1057520298(A;A) rs1057520298(C;C)
Reference Rs1057520298(G;G)
Significance Pathogenic
Disease not provided Wieacker syndrome
Variation info
Gene ZC4H2
CLNDBN not provided Wieacker syndrome
Reversed 1
HGVS NC_000023.10:g.64141692C>G; NC_000023.10:g.64141692C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000489055.1, RCV000444927.1,