Original source

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


Chromosome 14: between 35402236 and 35402237 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs147444522

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 22 transcripts and has 1 sample genotype.

Variant displays