Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.05 (T)
Location

Chromosome 11:120235377 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61000713

HGVS name

11:g.120235377G>T

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0

Variation displays