Original source

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

T/- | Ancestral: T | MAF: 0.45 (T)

Chromosome 5:68246331 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays