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: 0.09 (T)
Location

Chromosome X:37783152 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs34853679

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays