rs121909341

Orientation

plus

Stabilized

plus

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

Make rs121909341(A;A)

Make rs121909341(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

170108274

Gene

FOXI1

is a	snp
is	mentioned by
dbSNP	rs121909341
dbSNP (classic)	rs121909341
ClinGen	rs121909341
ebi	rs121909341
HLI	rs121909341
Exac	rs121909341
Gnomad	rs121909341
Varsome	rs121909341
LitVar	rs121909341
Map	rs121909341
PheGenI	rs121909341
Biobank	rs121909341
1000 genomes	rs121909341
hgdp	rs121909341
ensembl	rs121909341
geneview	rs121909341
scholar	rs121909341
google	rs121909341
pharmgkb	rs121909341
gwascentral	rs121909341
openSNP	rs121909341
23andMe	rs121909341
SNPshot	rs121909341
SNPdbe	rs121909341
MSV3d	rs121909341
GWAS Ctlg	rs121909341

Max Magnitude

0

OMIM	601093
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909341(A;A)
Alt	rs121909341(A;A)
Reference	Rs121909341(G;G)
Significance	Pathogenic
Disease	Enlarged vestibular aqueduct syndrome Pendred's syndrome
Variation	info
Gene	FOXI1
CLNDBN	Enlarged vestibular aqueduct syndrome Pendred's syndrome
Reversed	0
HGVS	NC_000005.9:g.169535278G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008965.2, RCV000008966.2,