Original source

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

Alleles
-/TGCCTAC/CTGCCTA
Location

Chromosome 8: between 118928263 and 118928264 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs375747838

This variation has 8 HGVS names - click the plus to show

Variation displays