Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.34 (G)
Location

Chromosome 1:231408034 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs849809

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 5022 sample genotypes and is mentioned in 4 citations.

Variant displays