Original source

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

Alleles
-/T/TT
Location

Chromosome 7: between 103594539 and 103594540 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature and has 6 sample genotypes.

Variant displays