Original source

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

-/A | MAF: 0.16 (A)

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

Most severe consequence
Evidence status


Archive dbSNP rs112178489, rs148909965

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

About this variant

This variant overlaps 4 transcripts and has 1095 individual genotypes.

Variation displays