Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909202

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909202(C;T)
Make rs121909202(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position71244662
GeneEYA1
is asnp
is mentioned by
dbSNPrs121909202
ebirs121909202
HLIrs121909202
Exacrs121909202
Varsomers121909202
Maprs121909202
PheGenIrs121909202
hapmaprs121909202
1000 genomesrs121909202
hgdprs121909202
ensemblrs121909202
gopubmedrs121909202
geneviewrs121909202
scholarrs121909202
googlers121909202
pharmgkbrs121909202
gwascentralrs121909202
openSNPrs121909202
23andMers121909202
23andMe allrs121909202
SNP Nexus

SNPshotrs121909202
SNPdbers121909202
MSV3drs121909202
GWAS Ctlgrs121909202
Max Magnitude0
OMIM601653
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121909202(T;T)
Alt rs121909202(T;T)
Reference rs121909202(C;C)
Significance Pathogenic
Disease Branchiootic syndrome Melnick-Fraser syndrome
Variation info
Gene EYA1
CLNDBN Branchiootic syndrome Melnick-Fraser syndrome
Reversed 1
HGVS NC_000008.10:g.72156897G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008405.2, RCV000008406.2,