This variant has been flagged

Variation has more than 3 different alleles

Original source

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

A/C/G/T | Ancestral: G | Ambiguity code: N | MAF: 0.48 (G)

Chromosome 1:155295386 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 9 transcripts, has 2598 sample genotypes and is mentioned in 1 citation.

Variant displays