rs769068305

Orientation

plus

Stabilized

plus

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

Make rs769068305(C;G)

Make rs769068305(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

209788614

Gene

IRF6

is a	snp
is	mentioned by
dbSNP	rs769068305
dbSNP (classic)	rs769068305
ClinGen	rs769068305
ebi	rs769068305
HLI	rs769068305
Exac	rs769068305
Gnomad	rs769068305
Varsome	rs769068305
LitVar	rs769068305
Map	rs769068305
PheGenI	rs769068305
Biobank	rs769068305
1000 genomes	rs769068305
hgdp	rs769068305
ensembl	rs769068305
geneview	rs769068305
scholar	rs769068305
google	rs769068305
pharmgkb	rs769068305
gwascentral	rs769068305
openSNP	rs769068305
23andMe	rs769068305
SNPshot	rs769068305
SNPdbe	rs769068305
MSV3d	rs769068305
GWAS Ctlg	rs769068305

Max Magnitude

0

ClinVar
Risk	rs769068305(G;G) rs769068305(T;T)
Alt	rs769068305(G;G) rs769068305(T;T)
Reference	Rs769068305(C;C)
Significance	Pathogenic
Disease	Van der Woude syndrome not provided
Variation	info
Gene	IRF6
CLNDBN	Van der Woude syndrome not provided
Reversed	0
HGVS	NC_000001.10:g.209961959C>T
CLNSRC
CLNACC	RCV000201948.1, RCV000430826.1,