Original source

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


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

Most severe consequence
Intron variant
Evidence status


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