Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.07 (G)
Location

Chromosome 14:102138013 (forward strand) | View in location tab

Co-located

with dbSNP rs201102946 (G/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60866357, rs1742625

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2507 sample genotypes.

Variant displays