Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)

Chromosome 2:47799328 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB MSH6_1345C_T_090610

HGVS names

This variant has 18 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 15 transcripts, 1 regulatory feature, has 2902 sample genotypes and is associated with 3 phenotypes.

Variant displays