rs281860306

Orientation

minus

Stabilized

minus

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

Make rs281860306(A;G)

Make rs281860306(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

69816327

Gene

FGF3

is a	snp
is	mentioned by
dbSNP	rs281860306
dbSNP (classic)	rs281860306
ClinGen	rs281860306
ebi	rs281860306
HLI	rs281860306
Exac	rs281860306
Gnomad	rs281860306
Varsome	rs281860306
LitVar	rs281860306
Map	rs281860306
PheGenI	rs281860306
Biobank	rs281860306
1000 genomes	rs281860306
hgdp	rs281860306
ensembl	rs281860306
geneview	rs281860306
scholar	rs281860306
google	rs281860306
pharmgkb	rs281860306
gwascentral	rs281860306
openSNP	rs281860306
23andMe	rs281860306
SNPshot	rs281860306
SNPdbe	rs281860306
MSV3d	rs281860306
GWAS Ctlg	rs281860306

Max Magnitude

0

ClinVar
Risk	rs281860306(G;G)
Alt	rs281860306(G;G)
Reference	Rs281860306(A;A)
Significance	Pathogenic
Disease	Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
Variation	info
Gene	FGF3
CLNDBN	Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
Reversed	1
HGVS	NC_000011.9:g.69631095T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022693.27,