Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.23 (C)
Location

Chromosome 10:100216744 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 2 HGVS names - click the plus to show

10:g.100216744G>C
ENST00000370397.7:c.933+1251C>G

This variation has assays on 5 chips - click the plus to show

Variation displays