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: 0.16 (A)
Location

Chromosome 1:11019901 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60982353

This variation has 21 HGVS names - click the plus to show

About this variant

This variant overlaps 34 transcripts and has 1104 individual genotypes.

Variation displays