Original source

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

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

Chromosome 3:171014539 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM951160

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2526 individual genotypes and is mentioned in 1 citation.

Variation displays