rs587776569

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(CACTAGCAAGCTGCTGGAC;CACTAGCAAGCTGCTGGAC)	0	common in clinvar
(CACTAGCAAGCTGCTGGACG;CACTAGCAAGCTGCTGGACG)	0	common in clinvar
(GTCCAGCAGCTTGCTAGTG;GTCCAGCAGCTTGCTAGTG)	0	common in clinvar

Make rs587776569(GTCCAGCAGCTTGCTAGTG;T)

Make rs587776569(T;T)

Reference

GRCh38 38.1/142

Chromosome

1

Position

209790667

Gene

IRF6

is a	snp
is	mentioned by
dbSNP	rs587776569
dbSNP (classic)	rs587776569
ClinGen	rs587776569
ebi	rs587776569
HLI	rs587776569
Exac	rs587776569
Gnomad	rs587776569
Varsome	rs587776569
LitVar	rs587776569
Map	rs587776569
PheGenI	rs587776569
Biobank	rs587776569
1000 genomes	rs587776569
hgdp	rs587776569
ensembl	rs587776569
geneview	rs587776569
scholar	rs587776569
google	rs587776569
pharmgkb	rs587776569
gwascentral	rs587776569
openSNP	rs587776569
23andMe	rs587776569
SNPshot	rs587776569
SNPdbe	rs587776569
MSV3d	rs587776569
GWAS Ctlg	rs587776569

Max Magnitude

0

ClinVar
Risk	Rs587776569(GTCCAGCAGCTTGCTAGTG;GTCCAGCAGCTTGCTAGTG) rs587776569(T;T)
Alt	Rs587776569(GTCCAGCAGCTTGCTAGTG;GTCCAGCAGCTTGCTAGTG) rs587776569(T;T)
Reference	Rs587776569(CACTAGCAAGCTGCTGGAC;CACTAGCAAGCTGCTGGAC)
Significance	Pathogenic
Disease	Van der Woude syndrome
Variation	info
Gene	IRF6
CLNDBN	Van der Woude syndrome
Reversed	1
HGVS	NC_000001.10:g.209964012_209964030del19insT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003581.5,