Original source

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

Alleles
-/G | MAF: 0.49 (G)
Location

Chromosome 14: between 36672783 and 36672784 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 HGVS names - click the plus to show

Variation displays