Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.22 (G)
Location

Chromosome 7:155253993 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS045643

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60350369, rs3808334

This variation has 2 HGVS names - click the plus to show

7:g.155253993G>A
ENST00000297375.4:c.686-1073G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays