Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 13:75552101 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57436711

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2579 individual genotypes.

Variation displays