Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.44 (A)
Location

Chromosome 4:102881422 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1269538

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2760 sample genotypes.

Variant displays