Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.11 (C)
Location

Chromosome 4:148436323 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030066

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

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

This variation has assays on 13 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 6313 individual genotypes and is mentioned in 17 citations.

Variation displays