Original source

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

Alleles
CC/-/TC
Location

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

Most severe consequence
Synonyms

Archive dbSNP rs367729020

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts.

Variation displays