Original source

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

Alleles
CC/-/TC
Location

Chromosome 4:9779768-9779769 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs367729020

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 6 transcripts.

Variant displays