Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.22 (G)
Location

Chromosome 18:5544831 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1617323

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

About this variant

This variant overlaps 14 transcripts and has 1104 individual genotypes.

Variation displays