Original source

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

-/T | MAF: 0.49 (-)

Chromosome 10: between 112951913 and 112951914 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs377427223, rs143225562

This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 1093 individual genotypes.

Variation displays