Human (GRCh37.p13)

This variant maps to 7 locations

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Alleles
T/A/C
Location

This variant maps to 7 genomic locations. Please select a location in the box above.

Evidence status

Synonyms

Archive dbSNP rs60766574, rs17505242

Genotyping chips

This variant has assays on 14 chips - Show

Original source

Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP

About this variant

This variant overlaps 1 regulatory feature, has 2504 sample genotypes, is associated with 35 phenotypes and is mentioned in 58 citations.

Description from SNPedia

rs7775228 is one of three HLA region SNPs used to tag the DQ2.2 haplotype in gs221. [PMID:18509540]... Show