Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/- | Ancestral: A | MAF: 0.12 (-)
Location

Chromosome 7:151572242 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2504 sample genotypes.

Variant displays