Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 1:45015006 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS982395

Most severe consequence
Clinical significance

Synonyms

LSDB 4805

This variation has 6 HGVS names - click the plus to show

1:g.45015006G>A
ENST00000472254.1:n.695G>A
ENST00000466193.1:n.468G>A
ENST00000465678.1:n.357G>A
ENST00000494399.3:n.1609G>A
ENST00000246337.6:c.942G>A

Variation displays