Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.39 (T)

Chromosome 1:75156931 (forward strand) | View in location tab


with COSMIC COSM3997664 (C/T)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs52800448, rs61235738

This variant has 3 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 4073 sample genotypes and is mentioned in 1 citation.

Variant displays