Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.17 (A)
Location

Chromosome 6:136999859 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59766138, rs1744050

HGVS name

6:g.136999859A>T

About this variant

This variant overlaps 5 transcripts and has 2510 sample genotypes.

Variant displays