rs587777737

Orientation

plus

Stabilized

plus

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

Make rs587777737(C;C)

Make rs587777737(C;T)

Reference

GRCh38 38.1/142

Chromosome

8

Position

101619632

Gene

GRHL2

is a	snp
is	mentioned by
dbSNP	rs587777737
dbSNP (classic)	rs587777737
ClinGen	rs587777737
ebi	rs587777737
HLI	rs587777737
Exac	rs587777737
Gnomad	rs587777737
Varsome	rs587777737
LitVar	rs587777737
Map	rs587777737
PheGenI	rs587777737
Biobank	rs587777737
1000 genomes	rs587777737
hgdp	rs587777737
ensembl	rs587777737
geneview	rs587777737
scholar	rs587777737
google	rs587777737
pharmgkb	rs587777737
gwascentral	rs587777737
openSNP	rs587777737
23andMe	rs587777737
SNPshot	rs587777737
SNPdbe	rs587777737
MSV3d	rs587777737
GWAS Ctlg	rs587777737

Max Magnitude

0

ClinVar
Risk	rs587777737(C;C)
Alt	rs587777737(C;C)
Reference	Rs587777737(T;T)
Significance	Pathogenic
Disease	Ectodermal dysplasia/short stature syndrome
Variation	info
Gene	GRHL2
CLNDBN	Ectodermal dysplasia/short stature syndrome
Reversed	0
HGVS	NC_000008.10:g.102631860T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000144237.3,