Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 13:19971246 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60165383

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

About this variant

This variant overlaps 5 transcripts and has 3 sample genotypes.

Variant displays