Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2510 sample genotypes.

Variant displays