Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)

Chromosome 13:75552101 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57436711

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2579 sample genotypes.

Variant displays