Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.02 (G)

Chromosome 2:165780477 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs4371368

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2775 sample genotypes.

Variant displays