Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.12 (A)

Chromosome 10:6045063 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60127900

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 4 transcripts, has 4062 sample genotypes and is mentioned in 1 citation.

Variant displays