Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 1:78408441 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM097741

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 17581

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays