Original source

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

T/- | Ancestral: T | MAF: 0.46 (-)

Chromosome 1:219917728 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57571974, rs147200304

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays