Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
-/GT/TG
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs67674945, rs141031319

HGVS names

This variant has 44 HGVS names - Show

About this variant

This variant overlaps 46 transcripts and has 1 sample genotype.

Variant displays