Original source

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

Alleles
-/CT | MAF: 0.42 (-)
Location

Chromosome 17: between 63498093 and 63498094 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60243473, rs143875197

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

About this variant

This variant overlaps 16 transcripts and has 2508 individual genotypes.

Variation displays