Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.18 (T)
Location

Chromosome 5:135032413 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61194069

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2737 sample genotypes and is mentioned in 1 citation.

Variant displays