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rs457717

From SNPedia

Orientationplus
Stabilizedplus
Make rs457717(A;A)
Make rs457717(A;G)
Make rs457717(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position76625147
GeneF2RL2, IQGAP2
is asnp
is mentioned by
dbSNPrs457717
ebirs457717
HLIrs457717
Exacrs457717
Varsomers457717
Maprs457717
PheGenIrs457717
hapmaprs457717
1000 genomesrs457717
hgdprs457717
ensemblrs457717
gopubmedrs457717
geneviewrs457717
scholarrs457717
googlers457717
pharmgkbrs457717
gwascentralrs457717
openSNPrs457717
23andMers457717
23andMe allrs457717
SNP Nexus

SNPshotrs457717
SNPdbers457717
MSV3drs457717
GWAS Ctlgrs457717
GMAF0.3935
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20068591OA-icon.png]
Trait Hearing impairment
Title A genome-wide association study for age-related hearing impairment in the Saami
Risk Allele T
P-val 4E-7
Odds Ratio None None
OMIM612976
Desc
Variant
Relatedalso


[PMID 26187738] The European GWAS-identified risk SNP rs457717 within IQGAP2 is not associated with age-related hearing impairment in Han male Chinese population