rs587777842

Orientation

plus

Stabilized

plus

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

Make rs587777842(A;A)

Make rs587777842(A;C)

Reference

GRCh38 38.1/142

Chromosome

7

Position

97024509

Gene

DLX5

is a	snp
is	mentioned by
dbSNP	rs587777842
dbSNP (classic)	rs587777842
ClinGen	rs587777842
ebi	rs587777842
HLI	rs587777842
Exac	rs587777842
Gnomad	rs587777842
Varsome	rs587777842
LitVar	rs587777842
Map	rs587777842
PheGenI	rs587777842
Biobank	rs587777842
1000 genomes	rs587777842
hgdp	rs587777842
ensembl	rs587777842
geneview	rs587777842
scholar	rs587777842
google	rs587777842
pharmgkb	rs587777842
gwascentral	rs587777842
openSNP	rs587777842
23andMe	rs587777842
SNPshot	rs587777842
SNPdbe	rs587777842
MSV3d	rs587777842
GWAS Ctlg	rs587777842

Max Magnitude

0

ClinVar
Risk	rs587777842(A;A)
Alt	rs587777842(A;A)
Reference	Rs587777842(C;C)
Significance	Pathogenic
Disease	Split-hand/foot malformation 1
Variation	info
Gene	DLX5
CLNDBN	Split-hand/foot malformation 1
Reversed	0
HGVS	NC_000007.13:g.96653821C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144533.2,