Original source

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

Alleles
-/G/T
Location

Chromosome 12: between 11668400 and 11668401 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs374384663

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 1 sample genotype.

Variant displays