Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 9:104822521 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM023598

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

9:g.104822521T>G
ENST00000374736.5:c.2803A>C
ENSP00000363868.3:p.Asn935His

Variation displays