Original source

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

Alleles
-/T/TT
Location

Chromosome 14: between 92096911 and 92096912 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs71123315

HGVS names

This variant has 100 HGVS names - Show

About this variant

This variant overlaps 102 transcripts and has 2 sample genotypes.

Variant displays