Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.22 (T)
Location

Chromosome 7:155461450 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS045644

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs3808333

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

This variation has assays on 4 chips - click the plus to show

Variation displays