Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R
Location

Chromosome 17:7675214 (forward strand)|View in location tab

Most severe consequence
 
Start lost
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 75 HGVS names - Show

About this variant

This variant overlaps 43 transcripts, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays