Original source

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

Alleles
-/C | MAF: 0.46 (-)
Location

Chromosome 15: between 42949600 and 42949601 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs140634913

This variation has 3 HGVS names - click the plus to show

Variation displays