Original source

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

Alleles
A/T|Ancestral: T|Ambiguity code: W|MAF: 0.22 (A)
Location

Chromosome 1:115294436 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 2900 sample genotypes and is mentioned in 1 citation.

Variant displays