Original source

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

Alleles
T/C/G | Ancestral: G | Ambiguity code: B | MAF: 0.23 (T)
Location

Chromosome 6:161515785 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs118125375, rs60603650

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts and has 2512 sample genotypes.

Variant displays