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rs1057520297

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520297(A;A)
Make rs1057520297(A;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position64921845
GeneZC4H2
is asnp
is mentioned by
dbSNPrs1057520297
dbSNP (old)rs1057520297
ClinGenrs1057520297
ebirs1057520297
HLIrs1057520297
Exacrs1057520297
Gnomadrs1057520297
Varsomers1057520297
Maprs1057520297
PheGenIrs1057520297
Biobankrs1057520297
1000 genomesrs1057520297
hgdprs1057520297
ensemblrs1057520297
gopubmedrs1057520297
geneviewrs1057520297
scholarrs1057520297
googlers1057520297
pharmgkbrs1057520297
gwascentralrs1057520297
openSNPrs1057520297
23andMers1057520297
23andMe allrs1057520297
SNPshotrs1057520297
SNPdbers1057520297
MSV3drs1057520297
GWAS Ctlgrs1057520297
Max Magnitude0
ClinVar
Risk rs1057520297(A;A)
Alt rs1057520297(A;A)
Reference Rs1057520297(T;T)
Significance Pathogenic
Disease Wieacker syndrome
Variation info
Gene ZC4H2
CLNDBN Wieacker syndrome
Reversed 1
HGVS NC_000023.10:g.64141725A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000425925.1,