Original source

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

Alleles
C/- | Ancestral: C
Location

Chromosome 16:31178121 (forward strand) | View in location tab

Co-located

with dbSNP rs12051357 (C/A/T)

Most severe consequence
HGVS name

16:g.31178121delC

About this variant

This variant overlaps 8 transcripts.

Variation displays