rs886039391

Orientation

minus

Stabilized

minus

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

Make rs886039391(C;T)

Make rs886039391(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

209790696

Gene

IRF6

is a	snp
is	mentioned by
dbSNP	rs886039391
dbSNP (classic)	rs886039391
ClinGen	rs886039391
ebi	rs886039391
HLI	rs886039391
Exac	rs886039391
Gnomad	rs886039391
Varsome	rs886039391
LitVar	rs886039391
Map	rs886039391
PheGenI	rs886039391
Biobank	rs886039391
1000 genomes	rs886039391
hgdp	rs886039391
ensembl	rs886039391
geneview	rs886039391
scholar	rs886039391
google	rs886039391
pharmgkb	rs886039391
gwascentral	rs886039391
openSNP	rs886039391
23andMe	rs886039391
SNPshot	rs886039391
SNPdbe	rs886039391
MSV3d	rs886039391
GWAS Ctlg	rs886039391

Max Magnitude

0

ClinVar
Risk	rs886039391(T;T)
Alt	rs886039391(T;T)
Reference	Rs886039391(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	IRF6
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.209964041G>A
CLNSRC
CLNACC	RCV000254748.1,