Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 14:102044389 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3183007

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 2 individual genotypes.

Variation displays