Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.31 (C)
Location

Chromosome 3:128765775 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60757577, rs66813696

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2505 sample genotypes.

Variant displays