Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.20 (T)
Location

Chromosome 3:123096820 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59798315

This variation has 8 HGVS names - click the plus to show

3:g.123096820T>C
ENST00000462833.1:c.1135-25392A>G
ENST00000470367.1:n.430-25392A>G
ENST00000491190.1:c.-109-9927A>G
ENST00000476455.1:c.-109-9927A>G
ENST00000466617.1:c.-189-25392A>G
ENST00000483566.1:c.-189-25392A>G
ENST00000309879.5:c.85-25392A>G

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip, Illumina_ExomeChip

Variation displays