Original source

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

C/G | Ambiguity code: S | MAF: 0.47 (C)

Chromosome 11:2314214 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs800141

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 2510 sample genotypes.

Variant displays