Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.27 (G)

Chromosome 20:5939435 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs538298, rs1296409

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2510 sample genotypes.

Variant displays