Original source

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

T/G | Ancestral: T | Ambiguity code: K | MAF: 0.01 (G)

Chromosome 17:63918814 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2505 sample genotypes and is mentioned in 1 citation.

Variant displays