Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.37 (T)
Location

Chromosome 11:8089993 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57969751

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

About this variant

This variant overlaps 3 transcripts, has 1382 individual genotypes and is mentioned in 5 citations.

Variation displays