Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.21 (C)

Chromosome 4:155211295 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60721603

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, has 2575 sample genotypes and is mentioned in 1 citation.

Variant displays