Original source

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

Alleles
-/G/GG|MAF: 0.21 (-)
Location

Chromosome 5: between 148071675 and 148071676 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 2515 sample genotypes.

Variant displays