rs869025279

Orientation

plus

Stabilized

plus

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

Make rs869025279(-;-)

Make rs869025279(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

49973766

Gene

DLX4

is a	snp
is	mentioned by
dbSNP	rs869025279
dbSNP (classic)	rs869025279
ClinGen	rs869025279
ebi	rs869025279
HLI	rs869025279
Exac	rs869025279
Gnomad	rs869025279
Varsome	rs869025279
LitVar	rs869025279
Map	rs869025279
PheGenI	rs869025279
Biobank	rs869025279
1000 genomes	rs869025279
hgdp	rs869025279
ensembl	rs869025279
geneview	rs869025279
scholar	rs869025279
google	rs869025279
pharmgkb	rs869025279
gwascentral	rs869025279
openSNP	rs869025279
23andMe	rs869025279
SNPshot	rs869025279
SNPdbe	rs869025279
MSV3d	rs869025279
GWAS Ctlg	rs869025279

Max Magnitude

0

ClinVar
Risk	rs869025279(-;-)
Alt	rs869025279(-;-)
Reference	Rs869025279(G;G)
Significance	Pathogenic
Disease	Orofacial cleft 15
Variation	info
Gene	DLX4
CLNDBN	Orofacial cleft 15
Reversed	0
HGVS	NC_000017.10:g.48051130delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000207311.1,