Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.43 (T)
Location

Chromosome 7:101323297 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59401454

HGVS name

7:g.101323297T>A

About this variant

This variant overlaps 11 transcripts and has 2594 individual genotypes.

Variation displays