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
Location

Chromosome 9:12695626 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971556

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 782, 2010_April_001_073_TYRP1_115501_0002

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

9:g.12695626C>G
ENST00000388918.6:c.497C>G
ENSP00000373570.4:p.Ser166Ter

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays