rs797044863

Orientation

minus

Stabilized

minus

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

Make rs797044863(C;T)

Make rs797044863(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

64921894

Gene

ZC4H2

is a	snp
is	mentioned by
dbSNP	rs797044863
dbSNP (classic)	rs797044863
ClinGen	rs797044863
ebi	rs797044863
HLI	rs797044863
Exac	rs797044863
Gnomad	rs797044863
Varsome	rs797044863
LitVar	rs797044863
Map	rs797044863
PheGenI	rs797044863
Biobank	rs797044863
1000 genomes	rs797044863
hgdp	rs797044863
ensembl	rs797044863
geneview	rs797044863
scholar	rs797044863
google	rs797044863
pharmgkb	rs797044863
gwascentral	rs797044863
openSNP	rs797044863
23andMe	rs797044863
SNPshot	rs797044863
SNPdbe	rs797044863
MSV3d	rs797044863
GWAS Ctlg	rs797044863

Max Magnitude

0

ClinVar
Risk	rs797044863(T;T)
Alt	rs797044863(T;T)
Reference	Rs797044863(C;C)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	ZC4H2
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000023.10:g.64141774G>A
CLNSRC
CLNACC	RCV000190667.1,