Original source

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

Alleles
-/A | MAF: 0.16 (A)
Location

Chromosome 4: between 41745132 and 41745133 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs112178489, rs148909965

This variation has 4 HGVS names - click the plus to show

Variation displays