Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.11 (C)
Location

Chromosome 10:81889983 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59962958

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

10:g.81889983T>C
ENST00000602794.3:c.*371+318T>C
ENST00000555784.3:c.135+11888T>C
ENST00000404576.4:c.135+11888T>C
ENST00000404547.3:c.823+13820T>C
ENST00000556918.3:c.135+11888T>C
ENST00000372142.4:c.60+11963T>C
ENST00000372141.4:c.823+13820T>C

This variation has assays on 6 chips - click the plus to show

Variation displays