rs104893884

Orientation

minus

Stabilized

minus

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

Make rs104893884(C;T)

Make rs104893884(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

44305045

Gene

FGF10

is a	snp
is	mentioned by
dbSNP	rs104893884
dbSNP (classic)	rs104893884
ClinGen	rs104893884
ebi	rs104893884
HLI	rs104893884
Exac	rs104893884
Gnomad	rs104893884
Varsome	rs104893884
LitVar	rs104893884
Map	rs104893884
PheGenI	rs104893884
Biobank	rs104893884
1000 genomes	rs104893884
hgdp	rs104893884
ensembl	rs104893884
geneview	rs104893884
scholar	rs104893884
google	rs104893884
pharmgkb	rs104893884
gwascentral	rs104893884
openSNP	rs104893884
23andMe	rs104893884
SNPshot	rs104893884
SNPdbe	rs104893884
MSV3d	rs104893884
GWAS Ctlg	rs104893884

GMAF

0.0004591

Max Magnitude

0

OMIM	602115
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893884(G;G) rs104893884(T;T)
Alt	rs104893884(G;G) rs104893884(T;T)
Reference	Rs104893884(C;C)
Significance	Pathogenic
Disease	Congenital absence of salivary gland
Variation	info
Gene	FGF10
CLNDBN	Congenital absence of salivary gland
Reversed	1
HGVS	NC_000005.9:g.44305147G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007964.4,