Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W
Location

Chromosome 10:112956367 (forward strand)|View in location tab

Co-located variant

dbSNP rs10711698 (T/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 1 sample genotype.

Variant displays