Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)
Location

Chromosome 8:97172796 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

8:g.97172796C>A
ENST00000287020.5:c.125G>T
ENSP00000287020.4:p.Gly42Val

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays