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: 0.02 (G)
Location

Chromosome 5:174724643 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

LSDB NM_002449.4:c.-17C>G

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, has 1095 individual genotypes and is mentioned in 1 citation.

Variation displays