Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.31 (A)
Location

Chromosome 3:37034946 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR045225

Most severe consequence
Evidence status

Synonyms

This variation has 4 HGVS names - click the plus to show

3:g.37034946G>A
ENST00000231790.2:c.-93G>A
LRG_216:g.5106G>A
LRG_216t1.1:c.-93G>A

This variation has assays on 8 chips - click the plus to show

Variation displays