Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.35 (C)
Location

Chromosome X:37792410 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17312240, rs34574976

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, has 1486 individual genotypes and is mentioned in 1 citation.

Variation displays