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Human (GRCh38.p14)

This variant maps to 2 locations

Select a location:
Alleles
G/A/C/T|MAF: 0.42 (C)
Location

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

Evidence status

Synonyms
Original source

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

About this variant

This variant has 505 sample genotypes and is mentioned in 23 citations.

Description from SNPedia

Description not available [More information from SNPedia]