Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.48 (C)
Location

Chromosome 16:56961324 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR000229

Most severe consequence
Evidence status

Synonyms
HGVS name

16:g.56961324C>A

This variation has assays on 15 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2562 individual genotypes, is associated with 7 phenotypes and is mentioned in 54 citations.

Variation displays