Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.27 (A)
Location

Chromosome 16:89755903 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57123318

This variation has 17 HGVS names - click the plus to show

16:g.89755903A>G
ENST00000512912.1:c.*105-1058A>G
ENST00000472018.1:n.171+171A>G
ENST00000504473.1:n.364-1058A>G
ENST00000503560.1:n.457+171A>G
ENST00000505733.1:n.181+171A>G
ENST00000502547.1:c.*177+171A>G
ENST00000511415.1:c.*51+171A>G
ENST00000510811.2:c.88-1058A>G
ENST00000564192.1:c.-54+171A>G
ENST00000508723.1:c.*220+171A>G
ENST00000507205.1:n.123+189A>G
ENST00000505473.1:c.-54+171A>G
ENST00000378277.4:n.86-1058A>G
ENST00000331006.8:c.20-1058A>G
ENST00000353379.7:c.160+171A>G
ENST00000514965.1:n.332+171A>G

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

Variation displays