Original source

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

TA/- | MAF: 0.15 (-)

Chromosome 13:23213754-23213755 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs141802795

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2508 sample genotypes.

Variant displays