Original source

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

Alleles
-/G
Location

Chromosome 16: between 23365620 and 23365621 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs149626590, rs59922401

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts.

Variant displays