Original source

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

-/GCT|MAF: 0.46 (GCT)

Chromosome 11: between 120267644 and 120267645 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs147304777

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2513 sample genotypes.

Variant displays