rs104894955

Orientation

minus

Stabilized

minus

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

Make rs104894955(C;T)

Make rs104894955(T;T)

Reference

GRCh38 38.1/142

Chromosome

X

Position

47449438

Gene

ZNF41

is a	snp
is	mentioned by
dbSNP	rs104894955
dbSNP (classic)	rs104894955
ClinGen	rs104894955
ebi	rs104894955
HLI	rs104894955
Exac	rs104894955
Gnomad	rs104894955
Varsome	rs104894955
LitVar	rs104894955
Map	rs104894955
PheGenI	rs104894955
Biobank	rs104894955
1000 genomes	rs104894955
hgdp	rs104894955
ensembl	rs104894955
geneview	rs104894955
scholar	rs104894955
google	rs104894955
pharmgkb	rs104894955
gwascentral	rs104894955
openSNP	rs104894955
23andMe	rs104894955
SNPshot	rs104894955
SNPdbe	rs104894955
MSV3d	rs104894955
GWAS Ctlg	rs104894955

Max Magnitude

0

OMIM	314995
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894955(T;T)
Alt	rs104894955(T;T)
Reference	Rs104894955(C;C)
Significance	Probable-non-pathogenic
Disease	not provided Non-syndromic X-linked intellectual disability
Variation	info
Gene	ZNF41
CLNDBN	not provided Non-syndromic X-linked intellectual disability
Reversed	1
HGVS	NC_000023.10:g.47308837G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000088660.2, RCV000295327.1,