Original source

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

Alleles
TT/-
Location

Chromosome 1:150693848-150693849 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs72035116, rs66627373

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 1 sample genotype.

Variant displays