Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2513 sample genotypes.

Variant displays