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 2:128183690 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM951003

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays