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. 2013 Dec 10;2013:238528. doi: 10.1155/2013/238528

Table 2.

Allele frequencies.

Gene Reference SNP ID Genotype Our study (n = 103) HWE
P
HapmapJPT
(n = 172)
P GeMDBJ(MTHFR c.677C>T: n = 2,375 
MTHFR c.1298A>C: n = 1,428 
SLCO1B1 c.521T>C: n = 1,427)
P
MTHFR  c.677 C>T rs1801133 CC 32 68 864
CT 61 84 1123
TT 10 0.049 20 0.442 388 0.885

MTHFR  c.1298 A>C rs1801131 AA 68 112 952
AC 31 56 435
CC 4 0.633 4 0.924 41 0.765

SLCO1B1 rs11045879 TT 42 70 n.d.
TC 43 74 n.d.
CC 18 0.495 28 0.896 n.d. n.d.

SLCO1B1  c.521 T>C rs4149056 TT 73 138 1048
TC 26 30 347
CC 4 0.686 4 0.066 32 0.408

Difference of each allele frequency was calculated by  χ 2  test.

NCBI Hapmap JPT: database at National Center of Biotechnology Information (http://www.ncbi.nlm.nih.gov/).

The submitted SNP numbers to NCBI were ss65837366 for MTHFR C677T, ss76885974 for MTHFR A1298C, ss15510724 for SLCO1B1 rs11045879, and ss105439952 for SLCO1B1 T521C.

GeMDBJ: Genome Medicine Database of Japan (https://gemdbj.nibio.go.jp/dgdb/index.do).