Original source

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

Alleles
-/G/T/TGT
Location

Chromosome 5: between 148095950 and 148095951 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs142972606

HGVS names

This variant has 30 HGVS names - Show

About this variant

This variant overlaps 27 transcripts and has 2 sample genotypes.

Variant displays