Original source

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

Alleles
-/T | MAF: 0.49 (-)
Location

Chromosome 10: between 114711672 and 114711673 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs377427223, rs143225562

This variation has 14 HGVS names - click the plus to show

Variation displays