rs1057520298

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1057520298(A;A)

Make rs1057520298(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

64921812

Gene

ZC4H2

is a	snp
is	mentioned by
dbSNP	rs1057520298
dbSNP (classic)	rs1057520298
ClinGen	rs1057520298
ebi	rs1057520298
HLI	rs1057520298
Exac	rs1057520298
Gnomad	rs1057520298
Varsome	rs1057520298
LitVar	rs1057520298
Map	rs1057520298
PheGenI	rs1057520298
Biobank	rs1057520298
1000 genomes	rs1057520298
hgdp	rs1057520298
ensembl	rs1057520298
geneview	rs1057520298
scholar	rs1057520298
google	rs1057520298
pharmgkb	rs1057520298
gwascentral	rs1057520298
openSNP	rs1057520298
23andMe	rs1057520298
SNPshot	rs1057520298
SNPdbe	rs1057520298
MSV3d	rs1057520298
GWAS Ctlg	rs1057520298

Max Magnitude

0

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,