Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.12 (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 4917 individual genotypes and is mentioned in 15 citations.

Variation displays