rs104893835

Orientation

minus

Stabilized

minus

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

Make rs104893835(C;T)

Make rs104893835(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

13819120

Gene

WNT7A

is a	snp
is	mentioned by
dbSNP	rs104893835
dbSNP (classic)	rs104893835
ClinGen	rs104893835
ebi	rs104893835
HLI	rs104893835
Exac	rs104893835
Gnomad	rs104893835
Varsome	rs104893835
LitVar	rs104893835
Map	rs104893835
PheGenI	rs104893835
Biobank	rs104893835
1000 genomes	rs104893835
hgdp	rs104893835
ensembl	rs104893835
geneview	rs104893835
scholar	rs104893835
google	rs104893835
pharmgkb	rs104893835
gwascentral	rs104893835
openSNP	rs104893835
23andMe	rs104893835
SNPshot	rs104893835
SNPdbe	rs104893835
MSV3d	rs104893835
GWAS Ctlg	rs104893835

Max Magnitude

0

OMIM	601570
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893835(T;T)
Alt	rs104893835(T;T)
Reference	Rs104893835(C;C)
Significance	Pathogenic
Disease	Ulna and fibula absence of with severe limb deficiency
Variation	info
Gene	WNT7A
CLNDBN	Ulna and fibula absence of with severe limb deficiency
Reversed	1
HGVS	NC_000003.11:g.13860617G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008526.3,