Original source

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

Alleles
-/G | MAF: 0.22 (-)
Location

Chromosome 5: between 148071675 and 148071676 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 1103 individual genotypes.

Variation displays