Original source

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

Alleles
C/T | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 17:27756320 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.27756320C>T

About this variant

This variant overlaps 3 transcripts and has 2567 individual genotypes.

Variation displays