Original source

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

A/T | Ancestral: A | Ambiguity code: W | MAF: 0.02 (T)

Chromosome 1:167263573 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2504 sample genotypes and is mentioned in 1 citation.

Variant displays