rs587777093

Orientation

plus

Stabilized

plus

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

Make rs587777093(A;A)

Make rs587777093(A;G)

Reference

GRCh38 38.1/142

Chromosome

9

Position

128634259

Gene

WDR34

is a	snp
is	mentioned by
dbSNP	rs587777093
dbSNP (classic)	rs587777093
ClinGen	rs587777093
ebi	rs587777093
HLI	rs587777093
Exac	rs587777093
Gnomad	rs587777093
Varsome	rs587777093
LitVar	rs587777093
Map	rs587777093
PheGenI	rs587777093
Biobank	rs587777093
1000 genomes	rs587777093
hgdp	rs587777093
ensembl	rs587777093
geneview	rs587777093
scholar	rs587777093
google	rs587777093
pharmgkb	rs587777093
gwascentral	rs587777093
openSNP	rs587777093
23andMe	rs587777093
SNPshot	rs587777093
SNPdbe	rs587777093
MSV3d	rs587777093
GWAS Ctlg	rs587777093

Max Magnitude

0

ClinVar
Risk	rs587777093(A;A)
Alt	rs587777093(A;A)
Reference	Rs587777093(G;G)
Significance	Pathogenic
Disease	Short-rib thoracic dysplasia 11 with or without polydactyly
Variation	info
Gene	WDR34
CLNDBN	Short-rib thoracic dysplasia 11 with or without polydactyly
Reversed	0
HGVS	NC_000009.11:g.131396538G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000083285.4,