Original source

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

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

Chromosome 4:148435200 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 3468 individual genotypes and is mentioned in 2 citations.

Variation displays