Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.18 (C)
Location

Chromosome 7:97020044 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

7:g.97020044A>C

This variation has assays on 12 chips - click the plus to show

Variation displays