rs1060499555

Orientation

minus

Stabilized

minus

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

Make rs1060499555(C;C)

Make rs1060499555(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

209801301

Gene

IRF6

is a	snp
is	mentioned by
dbSNP	rs1060499555
dbSNP (classic)	rs1060499555
ClinGen	rs1060499555
ebi	rs1060499555
HLI	rs1060499555
Exac	rs1060499555
Gnomad	rs1060499555
Varsome	rs1060499555
LitVar	rs1060499555
Map	rs1060499555
PheGenI	rs1060499555
Biobank	rs1060499555
1000 genomes	rs1060499555
hgdp	rs1060499555
ensembl	rs1060499555
geneview	rs1060499555
scholar	rs1060499555
google	rs1060499555
pharmgkb	rs1060499555
gwascentral	rs1060499555
openSNP	rs1060499555
23andMe	rs1060499555
SNPshot	rs1060499555
SNPdbe	rs1060499555
MSV3d	rs1060499555
GWAS Ctlg	rs1060499555

Max Magnitude

0

ClinVar
Risk	rs1060499555(C;C)
Alt	rs1060499555(C;C)
Reference	Rs1060499555(T;T)
Significance	Pathogenic
Disease	Van der Woude syndrome
Variation	info
Gene	IRF6
CLNDBN	Van der Woude syndrome
Reversed	1
HGVS	NC_000001.10:g.209974646A>G
CLNSRC
CLNACC	RCV000449637.1,