rs104893635

Orientation

plus

Stabilized

plus

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

Make rs104893635(A;G)

Make rs104893635(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

176094672

Gene

HOXD13

is a	snp
is	mentioned by
dbSNP	rs104893635
dbSNP (classic)	rs104893635
ClinGen	rs104893635
ebi	rs104893635
HLI	rs104893635
Exac	rs104893635
Gnomad	rs104893635
Varsome	rs104893635
LitVar	rs104893635
Map	rs104893635
PheGenI	rs104893635
Biobank	rs104893635
1000 genomes	rs104893635
hgdp	rs104893635
ensembl	rs104893635
geneview	rs104893635
scholar	rs104893635
google	rs104893635
pharmgkb	rs104893635
gwascentral	rs104893635
openSNP	rs104893635
23andMe	rs104893635
23andMe all	rs104893635
SNPshot	rs104893635
SNPdbe	rs104893635
MSV3d	rs104893635
GWAS Ctlg	rs104893635

Max Magnitude

0

OMIM	142989
Desc
Variant	0009
Related	also

ClinVar
Risk	rs104893635(G;G)
Alt	rs104893635(G;G)
Reference	Rs104893635(A;A)
Significance	Pathogenic
Disease	Syndactyly
Variation	info
Gene	HOXD13
CLNDBN	Syndactyly, type V
Reversed	0
HGVS	NC_000002.11:g.176959400A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016002.26,