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 6:161360193 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM035856

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2507 individual genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variation displays