Original source

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

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

Chromosome 9:107584802 (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.107584802T>G
ENST00000374736.3:c.2803A>C
ENSP00000363868.3:p.Asn935His

Variation displays