Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.33 (T)
Location

Chromosome 1:54645262 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59022236, rs56633835

This variation has 13 HGVS names - click the plus to show

1:g.54645262T>C
ENST00000311841.7:c.*178+4572A>G
ENST00000534324.1:c.541-237A>G
ENST00000493530.2:c.283-237A>G
ENST00000537208.1:c.540+4572A>G
ENST00000421415.1:c.*179-237A>G
ENST00000542737.1:c.541-237A>G
ENST00000528287.1:c.*179-237A>G
ENST00000420054.1:c.*535-237A>G
ENST00000419823.2:c.541-237A>G
ENST00000490863.1:n.2973-237A>G
ENST00000287899.8:c.540+4572A>G
ENST00000401046.3:c.97-237A>G

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

Variation displays