Original source

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

A/G | Ambiguity code: R | MAF: 0.01 (A)

Chromosome 10:133534029 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57753213

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2678 sample genotypes.

Variant displays