Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/G|Ancestral: G|Ambiguity code: K|MAF: 0.45 (G)
Location

Chromosome X:47026494 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57660987

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 3629 sample genotypes.

Variant displays