Original source

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

C/G | Ancestral: C | Ambiguity code: S

Chromosome 11:120267657 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs4285878, rs60107070

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 6 sample genotypes.

Variant displays