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rs10249788

From SNPedia

Orientationplus
Stabilizedplus
Make rs10249788(C;C)
Make rs10249788(C;T)
Make rs10249788(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position17298523
GeneAHR
is asnp
is mentioned by
dbSNPrs10249788
ebirs10249788
HLIrs10249788
Exacrs10249788
Varsomers10249788
Maprs10249788
PheGenIrs10249788
hapmaprs10249788
1000 genomesrs10249788
hgdprs10249788
ensemblrs10249788
gopubmedrs10249788
geneviewrs10249788
scholarrs10249788
googlers10249788
pharmgkbrs10249788
gwascentralrs10249788
openSNPrs10249788
23andMers10249788
23andMe allrs10249788
SNP Nexus

SNPshotrs10249788
SNPdbers10249788
MSV3drs10249788
GWAS Ctlgrs10249788
GMAF0.2475
Max Magnitude

[PMID 23208493] Inhibition of AHR transcription by NF1C is affected by a single-nucleotide polymorphism, and is involved in suppression of human uterine endometrial cancer


[PMID 22211302] The association of functional polymorphisms in the aryl hydrocarbon receptor (AHR) gene with the risk of vitiligo in Han Chinese populations.