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rs1027557

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
(A;G) 0.1 heterozygosity seems common
Make rs1027557(G;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position130120384
is asnp
is mentioned by
dbSNPrs1027557
ebirs1027557
HLIrs1027557
Exacrs1027557
Varsomers1027557
Maprs1027557
PheGenIrs1027557
hapmaprs1027557
1000 genomesrs1027557
hgdprs1027557
ensemblrs1027557
gopubmedrs1027557
geneviewrs1027557
scholarrs1027557
googlers1027557
pharmgkbrs1027557
gwascentralrs1027557
openSNPrs1027557
23andMers1027557
23andMe allrs1027557
SNP Nexus

SNPshotrs1027557
SNPdbers1027557
MSV3drs1027557
GWAS Ctlgrs1027557
GMAF0.2893
Max Magnitude0.1
? (A;A) (A;G) (G;G) 28

This SNP, rs1027557, was mentioned as one of the SNPs defining a haplotype used during a search for a deafness-associated gene on chromosome 12. However, rs1027557 itself has no reported associations with deafness (or any other condition).


[PMID 16195816] Refinement of the DFNA41 locus and candidate genes analysis.