Original source

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

Alleles
A/G/T | Ancestral: A | Ambiguity code: D
Location

Chromosome 11:67490391 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM071538, CM106676

Most severe consequence
Clinical significance

Synonyms

LSDB NM_003977.2:c.721A>T, NM_003977.2:c.721A>G

This variation has 20 HGVS names - click the plus to show

Variation displays