Original source

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

A/G | Ancestral: A | Ambiguity code: R

Chromosome 4:1350697 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs3201437

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2 sample genotypes.

Variant displays