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rs161927

From SNPedia

Orientationplus
Stabilizedplus
Make rs161927(A;A)
Make rs161927(A;G)
Make rs161927(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position7796555
is asnp
is mentioned by
dbSNPrs161927
ebirs161927
HLIrs161927
Exacrs161927
Varsomers161927
Maprs161927
PheGenIrs161927
hapmaprs161927
1000 genomesrs161927
hgdprs161927
ensemblrs161927
gopubmedrs161927
geneviewrs161927
scholarrs161927
googlers161927
pharmgkbrs161927
gwascentralrs161927
openSNPrs161927
23andMers161927
23andMe allrs161927
SNP Nexus

SNPshotrs161927
SNPdbers161927
MSV3drs161927
GWAS Ctlgrs161927
GMAF0.1598
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20068591OA-icon.png] A genome-wide association study for age-related hearing impairment in the Saami
OMIM612976
Desc
Variant
Relatedalso