Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.08 (T)
Location

Chromosome 7:100722528 (forward strand) | View in location tab

Co-located

with dbSNP rs58566702 (-/CTCA)

Most severe consequence
Evidence status

Synonyms

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

Variation displays