Original source

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

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

Chromosome 16:46669007 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM115589

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB NM_018206.4:c.1570C>T

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts.

Variant displays