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: 0.20 (A)
Location

Chromosome 1:77926761 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 15 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts, has 2415 individual genotypes, is associated with 2 phenotypes and is mentioned in 2 citations.

Variation displays