This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ancestral: A | Ambiguity code: N | MAF: 0.16 (A)
Location

Chromosome 7:39024584 (forward strand) | View in location tab

Co-located

with dbSNP rs113396099 (A/G)

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

Variation displays