Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 17:46805705 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

17:g.46805705C>T
ENST00000290295.7:c.251G>A
ENSP00000290295.7:p.Gly84Glu

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays