Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.50 (G)
Location

Chromosome 13:75579919 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60840295

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2903 sample genotypes.

Variant displays