Original source

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

C/A | Ancestral: C | Ambiguity code: M

Chromosome 17:65536345 (forward strand) | View in location tab

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 12342

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and is associated with 2 phenotypes.

Variant displays