Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M
Location

Chromosome 14:100835525 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs3194467

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and has 2 sample genotypes.

Variant displays