Original source

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

Alleles
-/A|MAF: 0.32 (A)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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