Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.22 (A)
Location

Chromosome 10:81896770 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57146204

This variation has 8 HGVS names - click the plus to show

10:g.81896770G>A
ENST00000602794.3:c.*371+7105G>A
ENST00000555784.3:c.135+18675G>A
ENST00000404547.3:c.823+20607G>A
ENST00000404576.4:c.135+18675G>A
ENST00000372142.4:c.60+18750G>A
ENST00000556918.3:c.135+18675G>A
ENST00000372141.4:c.823+20607G>A

This variation has assays on 10 chips - click the plus to show

Variation displays