Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: < 0.01 (G)
Location

Chromosome X:137567340 (forward strand) | View in location tab

Co-located

with COSMIC COSM32555 (C/G) ; HGMD-PUBLIC CM040505

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_373_ZIC3_300265_0007, 6972

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts, has 1092 individual genotypes, is associated with 3 phenotypes and is mentioned in 1 citation.

Variation displays