Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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