Original source

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

Alleles
-/AAAGAC/AC/CA|MAF: 0.49 (AAAGAC)
Location

Chromosome 7: between 101136456 and 101136457 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs139690533

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2504 sample genotypes.

Variant displays