Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.12 (C)

Chromosome 1:167287553 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60788541

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, has 2894 sample genotypes and is mentioned in 1 citation.

Variant displays