Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.16 (A)
Location

Chromosome 17:3939197 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

17:g.3939197G>A
ENST00000359983.4:c.2101-1561C>T
ENST00000397043.4:c.2101-1561C>T
ENST00000309890.8:c.2101-1561C>T
ENST00000397035.4:c.2101-1561C>T
ENST00000397041.4:c.2101-1561C>T
ENST00000352011.4:c.2101-1561C>T

This variation has assays on 4 chips - click the plus to show

Variation displays