rs536639583

Orientation

plus

Stabilized

plus

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

Make rs536639583(C;C)

Make rs536639583(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

176092922

Gene

HOXD13

is a	snp
is	mentioned by
dbSNP	rs536639583
dbSNP (classic)	rs536639583
ClinGen	rs536639583
ebi	rs536639583
HLI	rs536639583
Exac	rs536639583
Gnomad	rs536639583
Varsome	rs536639583
LitVar	rs536639583
Map	rs536639583
PheGenI	rs536639583
Biobank	rs536639583
1000 genomes	rs536639583
hgdp	rs536639583
ensembl	rs536639583
geneview	rs536639583
scholar	rs536639583
google	rs536639583
pharmgkb	rs536639583
gwascentral	rs536639583
openSNP	rs536639583
23andMe	rs536639583
SNPshot	rs536639583
SNPdbe	rs536639583
MSV3d	rs536639583
GWAS Ctlg	rs536639583

Max Magnitude

0

ClinVar
Risk	rs536639583(C;C)
Alt	rs536639583(C;C)
Reference	Rs536639583(G;G)
Significance	Pathogenic
Disease	Synpolydactyly 1 not specified
Variation	info
Gene	HOXD13
CLNDBN	Synpolydactyly 1 not specified
Reversed	0
HGVS	NC_000002.11:g.176957650G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000210944.2, RCV000489398.1,