Original source

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

Alleles
-/T/TT
Location

Chromosome 7: between 103858002 and 103858003 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs200006453, rs142568772

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 5 sample genotypes.

Variant displays