Original source

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


Chromosome 4: between 89809531 and 89809532 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs200957511

HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 22 transcripts and has 1 sample genotype.

Variant displays