Original source

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

Alleles
-/GT/TG
Location

Chromosome 14: between 100839948 and 100839949 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs67674945, rs141031319

This variant has 44 HGVS names - click the plus to show

About this variant

This variant overlaps 46 transcripts and has 1 sample genotype.

Variant displays