Original source

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

C/G | Ambiguity code: S | MAF: 0.27 (G)

Chromosome 6:10399924 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs74296083

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2521 sample genotypes.

Variant displays