Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.25 (T)
Location

Chromosome 6:160711114 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2581 sample genotypes.

Variant displays