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 1:97098598 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM973073

Most severe consequence
Evidence status

Clinical significance

This variation has 4 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 3 transcripts, has 2506 individual genotypes, is associated with 3 phenotypes and is mentioned in 3 citations.

Variation displays