Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: < 0.01 (C)
Location

Chromosome 14:64234135 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs59867117

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 2743 sample genotypes.

Variant displays