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Human (GRCh38.p14)

This variant maps to 2 locations

Select a location:
Alleles
T/A/C|MAF: 0.33 (C)
Location

This variant maps to 2 genomic locations. Please select a location in the box above.

Evidence status

Synonyms

Archive dbSNP rs58068500, rs17704184

Genotyping chips

This variant has assays on 10 chips - Show

Original source

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

About this variant

This variant has 2504 sample genotypes and is mentioned in 2 citations.