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: 0.35 (A)
Location

Chromosome 5:135027455 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs541059, rs59809179

HGVS name

5:g.135027455G>A

About this variant

This variant overlaps 6 transcripts and has 1102 individual genotypes.

Variation displays