Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

A/-|Ancestral: A

Chromosome 6:98837683 (forward strand)|View in location tab

Co-located variant

dbSNP rs751600284 (A/G)

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 11 sample genotypes.

Variant displays