Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.45 (C)
Location

Chromosome 5:1286401 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59399762

This variation has 7 HGVS names - click the plus to show

5:g.1286401C>A
ENST00000310581.7:c.1574-3777G>T
ENST00000508104.2:c.1574-3777G>T
ENST00000334602.8:c.1574-3777G>T
ENST00000460137.4:c.1574-3777G>T
LRG_343:g.13647G>T
LRG_343t1:c.1574-3777G>T

This variation has assays on 13 chips - click the plus to show

Variation displays