Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.17 (A)
Location

Chromosome 4:122408207 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61164551

This variation has 4 HGVS names - click the plus to show

4:g.122408207G>A
ENST00000296513.5:c.848+176G>A
ENST00000388724.5:c.848+176G>A
ENST00000388725.2:c.794+176G>A

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

About this variant

This variant overlaps 4 transcripts, has 2625 individual genotypes, is associated with 4 phenotypes and is mentioned in 23 citations.

Variation displays