Original source

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

-/A | MAF: 0.32 (A)

Chromosome 1: between 236797951 and 236797952 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs145816061, rs145201177

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2508 sample genotypes.

Variant displays