Original source

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

Alleles
T/-|Ancestral: T|MAF: 0.21 (-)
Location

Chromosome 1:113828177 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2507 sample genotypes.

Variant displays