Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: < 0.01 (C)

Chromosome 9:99144883 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB TGFBR1_1125A_C_112210

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts, has 2859 sample genotypes, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays