Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.36 (T)
Location

Chromosome 8:89760692 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59136347, rs2267541

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2511 individual genotypes.

Variation displays