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rs121909341

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909341(A;A)
Make rs121909341(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position170108274
GeneFOXI1
is asnp
is mentioned by
dbSNPrs121909341
ebirs121909341
HLIrs121909341
Exacrs121909341
Varsomers121909341
Maprs121909341
PheGenIrs121909341
hapmaprs121909341
1000 genomesrs121909341
hgdprs121909341
ensemblrs121909341
gopubmedrs121909341
geneviewrs121909341
scholarrs121909341
googlers121909341
pharmgkbrs121909341
gwascentralrs121909341
openSNPrs121909341
23andMers121909341
23andMe allrs121909341
SNP Nexus

SNPshotrs121909341
SNPdbers121909341
MSV3drs121909341
GWAS Ctlgrs121909341
Max Magnitude0
OMIM601093
Desc
Variant0002
Relatedalso
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,