rs121909574

Orientation

minus

Stabilized

minus

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

Make rs121909574(A;G)

Make rs121909574(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

10404509

Gene

TFAP2A

is a	snp
is	mentioned by
dbSNP	rs121909574
dbSNP (classic)	rs121909574
ClinGen	rs121909574
ebi	rs121909574
HLI	rs121909574
Exac	rs121909574
Gnomad	rs121909574
Varsome	rs121909574
LitVar	rs121909574
Map	rs121909574
PheGenI	rs121909574
Biobank	rs121909574
1000 genomes	rs121909574
hgdp	rs121909574
ensembl	rs121909574
geneview	rs121909574
scholar	rs121909574
google	rs121909574
pharmgkb	rs121909574
gwascentral	rs121909574
openSNP	rs121909574
23andMe	rs121909574
SNPshot	rs121909574
SNPdbe	rs121909574
MSV3d	rs121909574
GWAS Ctlg	rs121909574

Max Magnitude

0

OMIM	107580
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909574(C;C) rs121909574(G;G)
Alt	rs121909574(C;C) rs121909574(G;G)
Reference	Rs121909574(A;A)
Significance	Pathogenic
Disease	Branchiooculofacial syndrome
Variation	info
Gene	TFAP2A
CLNDBN	Branchiooculofacial syndrome
Reversed	1
HGVS	NC_000006.11:g.10404742T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019530.25,